Lab Tech - II
Job in
Waldorf, Charles County, Maryland, 20602, USA
Listed on 2026-01-11
Listing for:
Spectraforce Technologies
Full Time
position Listed on 2026-01-11
Job specializations:
-
Quality Assurance - QA/QC
-
Healthcare
Job Description & How to Apply Below
Job Title - Quality Control Technician I (QC Lab Support) Work Arrangement
Fredrick, MD 21704, 100% Onsite (Laboratory Environment)
Shift & Schedule- Day Shift: 4 days O 10 hours
- Sunday - Wednesday | 7:00 AM - 6:00 PM
12 Months
Role OverviewThe Quality Control Technician I - QC Lab Support is responsible for executing activities related to sample management, sample shipment, and laboratory support within the QC function. This role requires close cross-functional collaboration with Quality Assurance, Analytical Development, Manufacturing, Material Management (MM), Corporate QC
, and other QC teams to ensure compliant and efficient laboratory operations.
- Receive incoming samples, verify documentation, and log sample information into LIMS
. - Support sample receipt, processing, and aliquoting for release, stability testing, and retain samples.
- Label, store, organize, and maintain samples according to established procedures and storage requirements.
- Coordinate sample transfers to internal and external testing laboratories.
- Perform routine cleaning, maintenance, and restocking of sample storage areas.
- Collaborate with MM, QA, and QC functions
, including Corporate QC, to support sampling, testing, and disposition activities. - Manage and complete shipping activities within QC functions.
- Review and complete documentation, including chain-of-custody forms, processing logs, logbooks
, and other QC records. - Assist with deviations and investigations as needed.
- Provide updates during daily and weekly meetings
. - Participate in Lean Lab and other Operational Excellence initiatives.
- Ensure compliance with all safety, quality, and regulatory guidelines.
- Perform additional duties as assigned.
- Bachelor's Degree
, OR - Associate's Degree with 2+ years of experience in Quality Control or biopharma laboratories (FDA-regulated preferred), OR
- High School Diploma with 3+ years of experience in Quality Control or biopharma laboratories (FDA-regulated preferred).
- Strong knowledge of GMP application in a QC laboratory environment.
- Exceptional attention to detail and ability to manage multiple priorities.
- Proficiency in Microsoft Office
, Excel
, Visio
, and related applications. - Excellent interpersonal, verbal, and written communication skills in a collaborative environment.
- Comfortable working in a fast-paced
, small company environment with shifting priorities. - Flexible with schedule and willing to work overtime as needed
.
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